How are Lamivudine adverse event reports trending over time?
This graph shows volume of adverse events submitted to the FDA by quarter for Lamivudine, as well as related generic and/or brandname drugs containing the same primary active ingredients. Adverse events are counted if Lamivudine is flagged as the suspect drug causing the adverse event.
What are the most common Lamivudine adverse events reported to the FDA?
Drug Exposure During Pregnancy | 859 (3.05%) |
Immune Reconstitution Syndrome | 630 (2.24%) |
Pyrexia | 393 (1.4%) |
Vomiting | 302 (1.07%) |
Anaemia | 301 (1.07%) |
Nausea | 251 (.89%) |
Premature Baby | 240 (.85%) |
Alanine Aminotransferase Increased | 231 (.82%) |
Diarrhoea | 216 (.77%) |
Lactic Acidosis | 215 (.76%) |
Drug Ineffective | 204 (.73%) |
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This graph shows the top adverse events submitted to the FDA for Lamivudine, as well as related generic and/or brandname drugs containing the same primary active ingredients, from Q1 2004 to Q3 2012. Adverse events are counted if Lamivudine is flagged as a suspect drug causing the adverse event. For each adverse event listed, percent (%) represents percentage of the adverse event to all adverse events reported for the drug. Percent does not represent a rate related to drug utilization.
What are the most common Lamivudine adverse events reported to the FDA?
Hepatic And Hepatobiliary | 1501 (5.34%) |
Chemical Injury And Poisoning | 1132 (4.02%) |
Gastrointestinal Signs | 959 (3.41%) |
Hepatobiliary | 838 (2.98%) |
Epidermal And Dermal Conditions | 770 (2.74%) |
Infections - Pathogen Unspecified | 757 (2.69%) |
Therapeutic And Nontherapeutic Effe... | 682 (2.42%) |
Immunodeficiency Syndromes | 649 (2.31%) |
Respiratory | 596 (2.12%) |
Neurological | 595 (2.11%) |
Viral Infectious | 531 (1.89%) |
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This graph shows the top categories of adverse events submitted to the FDA for Lamivudine, as well as related generic and/or brandname drugs containing the same primary active ingredients, from Q1 2004 to Q3 2012. Adverse events are counted if Lamivudine is flagged as a suspect drug causing the adverse event. For each adverse event listed, percent (%) represents percentage of the adverse event to all adverse events reported for the drug. Percent does not represent a rate related to drug utilization.
Why are people taking Lamivudine, according to those reporting adverse events to the FDA?
Hiv Infection | 6435 |
Drug Exposure During Pregnancy | 577 |
Hepatitis B | 500 |
Drug Use For Unknown Indication | 461 |
Antiretroviral Therapy | 380 |
Acquired Immunodeficiency Syndrome | 264 |
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Label | Labeler | Effective |
---|---|---|
Combivir | Stat Rx USA | 27-OCT-09 |
Epivir | State of Florida DOH Central Pharmacy | 13-APR-10 |
Epivir | Physicians Total Care, Inc. | 14-APR-10 |
Epzicom | State of Florida DOH Central Pharmacy | 11-MAY-10 |
Epzicom | Physicians Total Care, Inc. | 01-JUL-10 |
Epivir | Rebel Distributors Corp | 24-SEP-10 |
Combivir | Rebel Distributors Corp | 24-SEP-10 |
Epzicom | GlaxoSmithKline LLC | 11-JAN-11 |
Epivir | GlaxoSmithKline LLC | 11-JAN-11 |
Combivir | GlaxoSmithKline LLC | 14-MAR-11 |
Combivir | PD-Rx Pharmaceuticals, Inc. | 14-MAR-11 |
Epivir | KAISER FOUNDATION HOSPITALS | 31-MAR-11 |
Trizivir | GlaxoSmithKline LLC | 13-JUL-11 |
Lamivudine | Apotex Corp. | 30-JUL-11 |
Epivirhbv | GlaxoSmithKline LLC | 13-DEC-11 |
Lamivudine And Zidovudine | PD-Rx Pharmaceuticals, Inc. | 23-DEC-11 |
Combivir | HHS/Program Support Center/Supply Service Center | 03-JAN-12 |
Lamivudine | Golden State Medical Supply, Inc. | 09-JAN-12 |
Combivir | H.J. Harkins Company, Inc. | 02-FEB-12 |
Lamivudine | American Health Packaging | 15-MAR-12 |
Lamivudine And Zidovudine | Rebel Distributors Corp | 04-APR-12 |
Lamivudine | Aurobindo Pharma Limited | 20-APR-12 |
Lamivudine And Zidovudine | Lupin Pharmaceuticals, Inc. | 24-APR-12 |
Lamivudine And Zidovudine | Aurobindo Pharma Limited | 15-MAY-12 |
Epzicom | ViiV Healthcare Company | 18-MAY-12 |
Lamivudine And Zidovudine | Teva Pharmaceuticals USA Inc | 21-MAY-12 |
Trizivir | ViiV Healthcare Company | 22-MAY-12 |
Lamivudine And Zidovudine | H.J. Harkins Company, Inc. | 25-JUN-12 |
Lamivudine And Zidovudine | St Marys Medical Park Pharmacy | 29-AUG-12 |
Epivir | Bryant Ranch Prepack | 12-OCT-12 |
Combivir | ViiV Healthcare Company | 16-JAN-13 |
Lamivudine And Zidovudine | Bryant Ranch Prepack | 18-JAN-13 |
Epivir | ViiV Healthcare Company | 23-JAN-13 |
Combivir | REMEDYREPACK INC. | 11-MAR-13 |
Epivir | REMEDYREPACK INC. | 15-MAR-13 |
Epzicom | REMEDYREPACK INC. | 15-MAR-13 |
Lamivudine | REMEDYREPACK INC. | 28-MAR-13 |
Lamivudine And Zidovudine | REMEDYREPACK INC. | 11-APR-13 |
Lamivudine | REMEDYREPACK INC. | 11-APR-13 |
Lamivudine | REMEDYREPACK INC. | 11-APR-13 |
Lamivudine And Zidovudine | REMEDYREPACK INC. | 11-APR-13 |
Lamivudine | REMEDYREPACK INC. | 11-APR-13 |
Combivir | REMEDYREPACK INC. | 23-APR-13 |
Combivir | REMEDYREPACK INC. | 23-APR-13 |
Combivir | REMEDYREPACK INC. | 23-APR-13 |
What Lamivudine safety concerns are being reported by doctors and researchers in the medical literature?
This report contains aggregated drug side effects and adverse events for Lamivudine. The data has been pulled from the United States Food and Drug Administration's (US FDA) Adverse Event Reporting System (AERS), a database containing more than 4,000,000 adverse event reports.
DrugCite expands your query using the Unified Medical Language System (UMLS) to include generic drugs and primary active ingredients. While the core of DrugCite's advanced drug filtering algorithm is based on the industry standard UMLS, DrugCite's proprietary filtering system also includes dozens of additional steps to reconcile malformed drug names in the FDA's data.
DrugCite only counts a drug if the submitter of the adverse event indicates that the drug is suspected to have caused the adverse event.
Depending on how the data is aggregated, different counts may occur. When someone submits an adverse event to the FDA, the submitter can attribute multiple adverse events to one or more drugs. For example, an individual taking Paxil could submit the adverse events "anxiety" and "suicidal ideation" for the same individual safety report (ISR). This means when DrugCite aggregates by adverse event, two distinct adverse events are counted in the adverse event graph; once for "anxiety" and again for "suicidal ideation". However, when DrugCite aggregates by individual safety reports irrespective of the details of the adverse events contained within the safety report, the report is only counted once.
Share your experience with Lamivudine.